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PharmaCompass offers a list of Irinotecan Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Irinotecan Hydrochloride manufacturer or Irinotecan Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Irinotecan Hydrochloride manufacturer or Irinotecan Hydrochloride supplier.
PharmaCompass also assists you with knowing the Irinotecan Hydrochloride API Price utilized in the formulation of products. Irinotecan Hydrochloride API Price is not always fixed or binding as the Irinotecan Hydrochloride Price is obtained through a variety of data sources. The Irinotecan Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 042LAQ1IIS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 042LAQ1IIS, including repackagers and relabelers. The FDA regulates 042LAQ1IIS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 042LAQ1IIS API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 042LAQ1IIS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 042LAQ1IIS supplier is an individual or a company that provides 042LAQ1IIS active pharmaceutical ingredient (API) or 042LAQ1IIS finished formulations upon request. The 042LAQ1IIS suppliers may include 042LAQ1IIS API manufacturers, exporters, distributors and traders.
click here to find a list of 042LAQ1IIS suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The 042LAQ1IIS Drug Master File in Japan (042LAQ1IIS JDMF) empowers 042LAQ1IIS API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the 042LAQ1IIS JDMF during the approval evaluation for pharmaceutical products. At the time of 042LAQ1IIS JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of 042LAQ1IIS suppliers with JDMF on PharmaCompass.
We have 7 companies offering 042LAQ1IIS
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